Canonical Allele Identifier: CA499671657

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143245679
• MyVariant Identifiers: chr17:g.37883667G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727414G>C , CM000679.2:g.39727414G>C	GRCh38
NC_000017.10:g.37883667G>C , CM000679.1:g.37883667G>C	GRCh37
NC_000017.9:g.35137193G>C	NCBI36
NG_007503.1:g.44275G>C , LRG_724:g.44275G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3279G>C MANE Select	ENSP00000269571.4:p.Gly1093=
ENST00000269571.9:c.3279G>C	ENSP00000269571.4:p.Gly1093=
ENST00000406381.6:c.3189G>C	ENSP00000385185.2:p.Gly1063=
ENST00000445658.6:c.2451G>C	ENSP00000404047.2:p.Gly817=
ENST00000541774.5:c.3234G>C	ENSP00000446466.1:p.Gly1078=
ENST00000578373.5:c.*3069G>C	ENSP00000463427.1:n.*3069G>C
ENST00000584450.5:c.3160-275G>C	ENSP00000463714.1:n.3160-275G>C
ENST00000584601.5:c.3189G>C	ENSP00000462438.1:p.Gly1063=
NM_001005862.2:c.3189G>C , LRG_724t1:c.3189G>C	NP_001005862.1:p.Gly1063=
NM_001289936.1:c.3234G>C , LRG_724t4:c.3234G>C	NP_001276865.1:p.Gly1078=
NM_001289937.1:c.3160-275G>C	NP_001276866.1:n.3160-275G>C
NM_004448.3:c.3279G>C , LRG_724t2:c.3279G>C	NP_004439.2:p.Gly1093=
NR_110535.1:n.3603G>C
XM_024450641.1:c.3417G>C	XP_024306409.1:p.Gly1139=
XM_024450642.1:c.3372G>C	XP_024306410.1:p.Gly1124=
XM_024450643.1:c.3327G>C	XP_024306411.1:p.Gly1109=
NM_001005862.3:c.3189G>C	NP_001005862.1:p.Gly1063=
NM_001289936.2:c.3234G>C	NP_001276865.1:p.Gly1078=
NM_001289937.2:c.3160-275G>C	NP_001276866.1:n.3160-275G>C
NM_001382782.1:c.3189G>C	NP_001369711.1:p.Gly1063=
NM_001382783.1:c.3189G>C	NP_001369712.1:p.Gly1063=
NM_001382784.1:c.3396G>C	NP_001369713.1:p.Gly1132=
NM_001382785.1:c.3381G>C	NP_001369714.1:p.Gly1127=
NM_001382786.1:c.3360G>C	NP_001369715.1:p.Gly1120=
NM_001382787.1:c.3354G>C	NP_001369716.1:p.Gly1118=
NM_001382788.1:c.3309G>C	NP_001369717.1:p.Gly1103=
NM_001382789.1:c.3300G>C	NP_001369718.1:p.Gly1100=
NM_001382790.1:c.3276G>C	NP_001369719.1:p.Gly1092=
NM_001382791.1:c.3270G>C	NP_001369720.1:p.Gly1090=
NM_001382792.1:c.3243G>C	NP_001369721.1:p.Gly1081=
NM_001382793.1:c.3237G>C	NP_001369722.1:p.Gly1079=
NM_001382794.1:c.3237G>C	NP_001369723.1:p.Gly1079=
NM_001382795.1:c.3231G>C	NP_001369724.1:p.Gly1077=
NM_001382796.1:c.3192G>C	NP_001369725.1:p.Gly1064=
NM_001382797.1:c.3180G>C	NP_001369726.1:p.Gly1060=
NM_001382798.1:c.3123G>C	NP_001369727.1:p.Gly1041=
NM_001382799.1:c.3099G>C	NP_001369728.1:p.Gly1033=
NM_001382800.1:c.3093G>C	NP_001369729.1:p.Gly1031=
NM_001382801.1:c.3075G>C	NP_001369730.1:p.Gly1025=
NM_001382802.1:c.3021G>C	NP_001369731.1:p.Gly1007=
NM_001382803.1:c.3118-275G>C	NP_001369732.1:n.3118-275G>C
NM_001382804.1:c.2451G>C	NP_001369733.1:p.Gly817=
NM_001382805.1:c.2328G>C	NP_001369734.1:p.Gly776=
NM_001382806.1:c.2241G>C	NP_001369735.1:p.Gly747=
NM_004448.4:c.3279G>C MANE Select	NP_004439.2:p.Gly1093=
NR_110535.2:n.3517G>C